A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961950



Internal ID22736889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128734144..128734144hg38UCSC Ensembl
chr9:131496423..131496423hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433610
Samples
Known GenesZER1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961950
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer